Canonical Allele Identifier: CA1465760708

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1731068035

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559717T>G , CM000666.2:g.68559717T>G	GRCh38
NC_000004.11:g.69425435T>G , CM000666.1:g.69425435T>G	GRCh37
NC_000004.10:g.69108030T>G	NCBI36
NG_017033.1:g.13811A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+820A>C (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+820A>C
ENST00000684088.1:c.255+820A>C (UGT2B17)	ENSP00000507374.1:n.255+820A>C
ENST00000317746.2:c.1005+820A>C (UGT2B17)	ENSP00000320401.2:n.1005+820A>C
ENST00000616841.4:c.1733-22191A>C (UGT2B15)	ENSP00000482004.1:n.1733-22191A>C
NM_001077.3:c.1005+820A>C (UGT2B17)	NP_001068.1:n.1005+820A>C
XM_024454205.1:c.1005+820A>C (UGT2B17)	XP_024309973.1:n.1005+820A>C
NM_001077.4:c.1005+820A>C (UGT2B17) MANE Select	NP_001068.1:n.1005+820A>C